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rs797044930

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044930(C;T)
Make rs797044930(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position13608697
GeneGRIN2B, LOC105369668
is asnp
is mentioned by
dbSNPrs797044930
ebirs797044930
HLIrs797044930
Exacrs797044930
Varsomers797044930
Maprs797044930
PheGenIrs797044930
hapmaprs797044930
1000 genomesrs797044930
hgdprs797044930
ensemblrs797044930
gopubmedrs797044930
geneviewrs797044930
scholarrs797044930
googlers797044930
pharmgkbrs797044930
gwascentralrs797044930
openSNPrs797044930
23andMers797044930
23andMe allrs797044930
SNP Nexus

SNPshotrs797044930
SNPdbers797044930
MSV3drs797044930
GWAS Ctlgrs797044930
Max Magnitude0
ClinVar
Risk rs797044930(T;T)
Alt rs797044930(T;T)
Reference rs797044930(C;C)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene GRIN2B
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000012.11:g.13761631G>A
CLNSRC
CLNACC RCV000190769.1,